Fan S T, Edgington T S
Department of Immunology, Research Institute of Scripps Clinic, La Jolla, CA 92037.
J Immunol. 1989 Dec 15;143(12):4287-91.
The origins of "help" in rejection of syngeneic tumors by the CD8 T cell lineage was examined with a model tumor inappropriately expressing novel class I MHC and subject to cytolytic T cell (CTL)-mediated rejection. The requirement for CD4+ Th cells to induce CD8+ CTL effectors in vivo was investigated by using C3H mice selectively depleted of either CD4+ or CD8+ T cells. Rejection of the tumor was vigorous and indistinguishable from normal mice after depletion of CD4+ T cells in vivo. In contrast, in CD8+ T cell-depleted mice tumors grew progressively, confirming that T cells of the CD8+ lineage are required for a tumoricidal immune response, and cells of this lineage are sufficient for a primary response. Taken together, these results demonstrate that, in the absence of CD4+ T cells in vivo, unprimed cells of the CD8+ lineage are fully competent to mount an effective CTL immune response to syngeneic cells expressing novel class I Ag, consistent with the concept that only T cells with class I recognition specificity may be required to satisfy the need for both help and effector functions in the response.
利用一种不适当表达新型I类主要组织相容性复合体(MHC)且易受细胞毒性T细胞(CTL)介导排斥的模型肿瘤,研究了CD8 T细胞谱系在排斥同基因肿瘤中“辅助”作用的起源。通过使用选择性清除CD4+或CD8+ T细胞的C3H小鼠,研究了体内诱导CD8+ CTL效应细胞对CD4+ Th细胞的需求。体内清除CD4+ T细胞后,肿瘤排斥反应强烈,与正常小鼠无异。相反,在CD8+ T细胞耗竭的小鼠中,肿瘤逐渐生长,证实CD8+谱系的T细胞是杀肿瘤免疫反应所必需的,且该谱系的细胞足以引发初次反应。综上所述,这些结果表明,在体内不存在CD4+ T细胞的情况下,未致敏的CD8+谱系细胞完全有能力对表达新型I类抗原的同基因细胞产生有效的CTL免疫反应,这与仅需具有I类识别特异性的T细胞就能满足反应中辅助和效应功能需求的概念一致。